2,6,12-Trihydroxy-7,11-dimethoxy-2,8-dimethyl-1,3,12,12a-tetrahydrotetracen-5-one

Details

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Internal ID a319a75c-bd99-4a1e-84bc-9513949c86fe
Taxonomy Benzenoids > Naphthalenes > Naphthols and derivatives
IUPAC Name 2,6,12-trihydroxy-7,11-dimethoxy-2,8-dimethyl-1,3,12,12a-tetrahydrotetracen-5-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H24O6/c1-10-5-6-12-14(20(10)27-3)19(25)15-16(21(12)28-4)18(24)13-9-22(2,26)8-7-11(13)17(15)23/h5-7,13,18,24-26H,8-9H2,1-4H3
InChI Key DLWWLZQHBLQMBR-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H24O6
Molecular Weight 384.40 g/mol
Exact Mass 384.15728848 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 2.90
Atomic LogP (AlogP) 3.19
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,6,12-Trihydroxy-7,11-dimethoxy-2,8-dimethyl-1,3,12,12a-tetrahydrotetracen-5-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.6615 66.15%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.8091 80.91%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9087 90.87%
OATP1B3 inhibitior + 0.9329 93.29%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.8287 82.87%
P-glycoprotein inhibitior - 0.4719 47.19%
P-glycoprotein substrate - 0.5606 56.06%
CYP3A4 substrate + 0.6498 64.98%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8218 82.18%
CYP3A4 inhibition - 0.7567 75.67%
CYP2C9 inhibition - 0.6850 68.50%
CYP2C19 inhibition + 0.5534 55.34%
CYP2D6 inhibition - 0.8792 87.92%
CYP1A2 inhibition + 0.5946 59.46%
CYP2C8 inhibition + 0.5388 53.88%
CYP inhibitory promiscuity - 0.6927 69.27%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8668 86.68%
Carcinogenicity (trinary) Non-required 0.5433 54.33%
Eye corrosion - 0.9924 99.24%
Eye irritation - 0.6348 63.48%
Skin irritation - 0.7463 74.63%
Skin corrosion - 0.9598 95.98%
Ames mutagenesis + 0.7082 70.82%
Human Ether-a-go-go-Related Gene inhibition - 0.5965 59.65%
Micronuclear - 0.5500 55.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.7610 76.10%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.7776 77.76%
Acute Oral Toxicity (c) III 0.3926 39.26%
Estrogen receptor binding + 0.8494 84.94%
Androgen receptor binding - 0.5628 56.28%
Thyroid receptor binding + 0.5726 57.26%
Glucocorticoid receptor binding + 0.8172 81.72%
Aromatase binding + 0.6024 60.24%
PPAR gamma + 0.7555 75.55%
Honey bee toxicity - 0.8430 84.30%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9951 99.51%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.52% 91.11%
CHEMBL240 Q12809 HERG 98.58% 89.76%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.96% 95.56%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 95.25% 92.68%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.88% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.86% 89.00%
CHEMBL2581 P07339 Cathepsin D 92.66% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.77% 99.23%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.61% 97.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.26% 94.00%
CHEMBL1937 Q92769 Histone deacetylase 2 87.45% 94.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.65% 86.33%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 85.79% 96.21%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.44% 95.89%
CHEMBL1871 P10275 Androgen Receptor 84.99% 96.43%
CHEMBL1951 P21397 Monoamine oxidase A 83.70% 91.49%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 83.50% 96.67%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 82.75% 93.03%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.42% 85.14%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 81.22% 89.62%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.63% 100.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.62% 93.99%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.03% 96.09%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Taxus cuspidata

Cross-Links

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PubChem 85147010
LOTUS LTS0272070
wikiData Q105018881